| Literature DB >> 29711013 |
Qiongzhong Jiang1, Yutong Jiang1, Dengming Xiao1, Ping Cao1, Xumu Zhang1.
Abstract
Even alkyl methyl ketones undergo asymmetric hydrogenation with high enantioselectivity when a rhodium complex of the conformationally rigid chiral ligand 1 (Me-PennPhos; R=CH3 ) is used as the catalyst. Basic additives such as 2,6-lutidine contribute to the achievement of high enantiomeric excesses. © 1998 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.Entities:
Keywords: Asymmetric catalysis; Chirality; Hydrogenations; Ketones; Rhodium
Year: 1998 PMID: 29711013 DOI: 10.1002/(SICI)1521-3773(19980504)37:8<1100::AID-ANIE1100>3.0.CO;2-3
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336